- Taiwan Oyi peptide Co. Ltd
- China
- Product Name: (Pro3)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt
- Price: $Inquiry/1mg $Inquiry/100kg
- Purity: 98.0%
- Stocking Period: 1 Day
- Contact: Vinnie
299898-52-5
299898-52-5 structure
- Name: (Pro3)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt
- Chemical Name: (Pro3)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt
- CAS Number: 299898-52-5
- Molecular Formula: C226H338N60O64S
- Molecular Weight:
- Catalog: Signaling Pathways Protein Tyrosine Kinase/RTK Insulin Receptor
- Create Date: 2021-01-07 22:43:44
- Modify Date: 2024-01-03 10:50:45
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(Pro3) GIP, human ((Pro3) Gastric Inhibitory Peptide, human) is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human has high binding affinity for human GIPR with Ki/ Kd values of 0.90 nM. (Pro3) GIP, human can be used for the research of obesity-related diabetes[1][2].
| Name | (Pro3)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt |
|---|
| Description | (Pro3) GIP, human ((Pro3) Gastric Inhibitory Peptide, human) is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human has high binding affinity for human GIPR with Ki/ Kd values of 0.90 nM. (Pro3) GIP, human can be used for the research of obesity-related diabetes[1][2]. |
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| Related Catalog | |
| Target |
EC50: 0.026 nM (hGIPR)[2] Ki/Kd: 0.90 nM (hGIPR); 1.1 nM (Rat GIPR); 0.72 nM (Mouse GIPR)[2] |
| In Vitro | (Pro3) GIP, human induces cAMP accumulation with an EC50 value of 0.026 nM[2]. (Pro3) GIP, human has high binding affinity for human GIPR, Rat GIPR and Mouse GIPR with Ki/ Kd values of 0.90 nM, 1.1 nM and 0.72 nM, respectively[2]. |
| In Vivo | (Pro3) GIP, human has comparatively weak partial agonist effect in rodent models[2]. |
| Molecular Formula | C226H338N60O64S |
|---|